The imprinted NPAP1/C15orf2 gene in the Prader-Willi syndrome region encodes a nuclear pore complex associated protein

✍ Scribed by Neumann, L. C.; Markaki, Y.; Mladenov, E.; Hoffmann, D.; Buiting, K.; Horsthemke, B.

• Book ID: 111904561
• Publisher: Oxford University Press
• Year: 2012
• Tongue: English
• Weight: 941 KB
• Volume: 21
• Category: Article
• ISSN: 0964-6906
• DOI: 10.1093/hmg/dds228